Endoscopic Ultrasound- Guided Hartmann Reversal Procedure
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorNicolaus Copernicus University
About this trial
The goal of this clinical trial is to learn about clinical usefulness endoscopic gastrointestinal anastomoses to restore the gastrointestinal continuity in patients with permanent colostomy after Hartmann procedure.
The main questions it aims to answer are:
* is the endoscopic restore the gastrointestinal continuity procedure effective? * is this endoscopic procedure safe?
Eligibility criteria
Qualifiers
participants of both sexes aged above 18 years
participants, who provided informed consent for such treatment
eligibility for Hartmann's procedure according to current medical knowledge based on evidence-based medicine.
Disqualifiers
pregnancy, breastfeeding, or intention to become pregnant during the study
contraindications to electrosurgical instruments
allergy to any of the materials used in the study
participants with advanced cancer in the metastatic stage
Trial design
Treatments tested in this trial
- Endoscopic restoration of gastrointestinal continuity after Hartmann procedure
Treatment groups
100 Participants
are divided into 1 treatment groupLocations
Sponsors and collaborators
Nicolaus Copernicus University
Lead sponsor
Medical University of Łódź
Collaborator
Source ClinicalTrials.gov